R & D Jobs in West Orange, New Jersey

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186 West Orange, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 186
LOOKING TO MAKE A MOVE TO CONSULTANCY? ANALYST / SENIOR ANALYST POSITION COMPANY PROFILE Medical Marketing Economics (MME) is a strategic advisory company to the global bio-pharmaceutical industry, focused on helping clients identify, frame, communicate and capture the value of their products while gaining timely and appropriate market access. We are driven by intellectual curiosity and are passio...
Type : Front-Line, Experienced Position Summary : The Principal Statistical Programmer is responsible for all programming aspects (including analysis datasets, pooled datasets, tables, listings, and figures) of individual Phase I – IV clinical trials and project level activities for drug/Life Science projects. The Principal Statistical Programmer provides technical expertise to offer consulting, t...
Key Activities : Statistical programming Providing support for creating and maintaining programs to analyze and report clinical trials data. o Create or review data specifications. o Program or validate derived datasets, tables, listings and graphs Providing quality control for study documents, programs and outputs of statistical programs Effectively contribute to department study teams. study Qua...
The incumbent will have the overall management and study site monitoring of clinical sites, which include conduct of pre-study and initiation visits, interim monitoring, and close out visits in accordance with company standard operating procedures. The incumbent will also have on and off-site monitoring responsibilities that include ensuring study staff has received proper training to conduct the...
We have been retained by one of the world's leading manufacturers of medical/surgical disposable products to assist them as they expand their sales organization. You will be responsible to manage your own N. New Jersey Territory for their existing business and develop new sales primarily in the acute care market. With products that are clinically superior, you will call on various departments of t...
PRINCIPAL SDTM PROGRAMMER *This remote opportunity is open to any US home-office location. Theorem Clinical Research is currently searching for experienced SDTM Programmers. In this role, the SDTM Programmer will be responsible for mapping entire studies in accordance with SDTM guidelines, as well as performing Quality Control checks. RESPONSIBILITIES: Create SAS datasets of clinical data from cli...
Seeking multiple Project Managers for consulting positions at a major pharmaceutical client in East Hanover, NJ 07936. Key components of the responsibilities are as mentioned below: · Manages projects from scope definition to deployment · Liaisons with internal and external client’s · Defines project scope, approach and understands client reporting requirements for adverse events · Creates strateg...
TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician(Some can be telecommute), Clinical Research Scientist/Clinical manager, Contract Specialists, Outsourcing Manager, Informed Consent Setup and study start up, Sr. Clinical Data Managerfor our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: *****...
Our client, a large pharmaceutical company, is currently seeking a DESKTOP PUBLISHER. Responsible for publishing and managing QC for high quality scientific documentation (e.g. study reports) for submission to regulatory authorities in support of marketing applications Preparation of high quality scientific documentation and submission documents in accordance with the timelines specified by NIBR a...
*BA/BS or advanced degree required! 3 years of experience required!* Duties: The team is looking for highly motivated and pleasant individuals with previous experience a clinical trial site in a global pharma company or those with experience in conducting a global study. We have a strong preference for those with a strong scientific or clinical background (i.e., oncology nurse, pharmacists, etc) a...
Hello, My name is Bryson Jackson and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Desktop Publisher (s) for a prominent client of ours. This position is located in East Hanover, NJ. Details for the positions are as follows: Job Description: LONG TERM CONTRACT!!!! FORTUNE 500 CLIENT!!!! Duties Responsible for publishing and managing QC for high quality...
Desktop Publisher – 6 month contract Responsible for publishing and managing QC for high quality scientific documentation (e.g. study reports) for submission to regulatory authorities in support of marketing applications. Preparation of high quality scientific documentation and submission documents in accordance with the timelines specified by Novartis Institutes for BioMedical Research (NIBR) and...
The Fountain Group has an IMMEDIATE opening for a Clinical Research Scientist in east Hanover, NJ. Qualified candidates should submit an updated resume along with contact information to be considered. Overview The team is looking for highly motivated and pleasant individual with previous experience at a clinical trial site in a global pharma company or those with experience in conducting a global...
Clinical Research Manager II – 6 month contract Support US efforts in the planning, execution and reporting of US Clinical Data and Medical Affairs (CDMA) clinical trials in Oncology: Implementation of clinical trials in the United States (safety, data consistency, trial timelines, budget, resources, eligibility and enrollment), within a cross functional team and with oversight from the Associate...
Biostatistician III – 6 month contract Designing clinical studies. Writing and reviewing statistical sections and other relevant parts of study synopses and protocols. Support study start up activities. Develop RAP, program TLFs, preparation for database lock, dry run and CSR activities. Review CRF, DB spec, VAP. Support analyses as required for decision making at project level. Support analyses a...
TechData is looking for Biostatistician (Contract/permanent, or remote), SAS Programmer/Statistical Programmer (Some can be telecommuting), Task Based Clinical Data Coordinator/Clinical Data Manager, CRS (Clinical Research Scientist, Clinical Scientist), Clinical Safety Scientist/Drug Safety for our pharmaceutical clients in Northern and Central NJ. Please see below requirements and send your resu...
Expert Clinical Manager III – 5 month contract Responsible for all operational aspects of 1 or more Office of Generic Drugs (OGD) clinical trial(s) under the leadership of Clinical Trial Head (CTH). Support all scientific aspects of clinical trial(s) as assigned. Responsible for program level activities as assigned. Ensure all operational trial deliverables are met according to timelines, budget,...
Minimum Requirements: Prior experience with Implementation of clinical trials in the United States safety, data consistency, trial timelines, budget, resources, eligibility and enrollment. Education: Bachelor Degree required Job Description: Support US efforts in the planning, execution and reporting of USCDMA clinical trials in Oncology. Implementation of clinical trials in the United States (saf...
TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician(Some can be telecommute), Clinical Research Scientist/Clinical manager, Contract Specialists, Outsourcing Manager, Informed Consent Setup and study start up, Sr. Clinical Data Managerfor our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: *****...
Founded in 1987, Canfield Scientific, Inc. is a core imaging lab providing custom photographic systems, image monitoring, and centralized analysis services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and supporting documentation. Canfield has supported over 2,000 clinical studies, worked worldwide with thousands o...
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